NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss106787101           
Submitter
HandleBGI
Submitter SNP IDBGI_rs10845281
RefSNP(rs#)rs10845281
Submitted Batch IDYanhuang1_20080807_a
Submitted DateSep 16, 2008
Publication CitedN.D.
First entry to dbSNPSep 16 2008 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodBGI-SEQUENCING
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleT/C
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss106787101|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
 ATTCCAAAAG CTTGGCAAAG CATTAAGACA ATTTCTTTTG GTAGCATCTT AGAATTCCAA
 AACGATATGA TTAGACACAG AAAGTAAATG GCAAGTAATA
 Y
 GAGGAAGGAG GTCACAGTTT GCAGAGCTTT TATGTGGATC TTGGTGCTGG GATCTTGAGA
 TCCTTTGCCA TGGAGCTGCA TCTTCTTCAG ATGTTTACAC

  Submitted Frequency for ss106787101 back to top
There is no frequency submission for ss106787101.


  dbSNP summary of Genotypes for ss106787101 back to top
No sufficient data to compute Hardy-weinberg probability for ss106787101.


  Submitted individual genotype for ss106787101 back to top
There is no individual genotype data for ss106787101.

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement